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FDA approval · 2023-12-21

FDA Approved: IDHIFA — Supplemental Application (Celgene Corporation)

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Summary

FDA approved a supplemental application for IDHIFA (enasidenib mesylate) to expand its labeling for acute myeloid leukemia with IDH2 mutation.

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Diseases / indications

Drugs mentioned

  • IDHIFA (enasidenib)

Snippet

SUPPL AP for IDHIFA (ENASIDENIB MESYLATE)